Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits. - Wikidata - wikimedia - TriplyDB

Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits.

Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits.

http://www.wikidata.org/entity/Q30422039

about

Insights into obesity and diabetes at the intersection of mouse and human genetics Association of novelty-related behaviors and intravenous cocaine self-administration in Diversity Outbred mice.Prediction of Causal Candidate Genes in Coronary Artery Disease Loci The Genetic Architecture of Hearing Impairment in Mice: Evidence for Frequency-Specific Genetic Determinants Trimethylamine-N-oxide, a metabolite associated with atherosclerosis, exhibits complex genetic and dietary regulation Collaborative Cross and Diversity Outbred data resources in the Mouse Phenome Database Hypothalamic transcriptomes of 99 mouse strains reveal trans eQTL hotspots, splicing QTLs and novel non-coding genes A Suite of Tools for Biologists That Improve Accessibility and Visualization of Large Systems Genetics Datasets: Applications to the Hybrid Mouse Diversity Panel.Large-scale phenotyping of noise-induced hearing loss in 100 strains of mice.The Genetic Architecture of Noise-Induced Hearing Loss: Evidence for a Gene-by-Environment Interaction Integration of genome-wide association and extant brain expression QTL identifies candidate genes influencing prepulse inhibition in inbred F1 mice.A Simplified, Langendorff-Free Method for Concomitant Isolation of Viable Cardiac Myocytes and Nonmyocytes From the Adult Mouse Heart.Bicc1 is a genetic determinant of osteoblastogenesis and bone mineral density.Genome-wide association study identifies nox3 as a critical gene for susceptibility to noise-induced hearing loss.Molecular nutrition research: the modern way of performing nutritional science Genome-wide association study for age-related hearing loss (AHL) in the mouse: a meta-analysis Fine-mapping QTLs in advanced intercross lines and other outbred populations.Genetic modulation of diabetic nephropathy among mouse strains with Ins2 Akita mutation.Epigenomes: the missing heritability in human cardiovascular disease?High-resolution genetic mapping in the diversity outbred mouse population identifies Apobec1 as a candidate gene for atherosclerosis.Dissecting impulsivity and its relationships to drug addictions.Combined QTL and selective sweep mappings with coding SNP annotation and cis-eQTL analysis revealed PARK2 and JAG2 as new candidate genes for adiposity regulation.Contrasting genetic architectures in different mouse reference populations used for studying complex traits.ASXL2 Regulates Glucose, Lipid, and Skeletal Homeostasis.Heritability of periodontal bone loss in mice.Nutritional systems biology of type 2 diabetes Nicotinamide N-methyltransferase regulates hepatic nutrient metabolism through Sirt1 protein stabilization.In-silico QTL mapping of postpubertal mammary ductal development in the mouse uncovers potential human breast cancer risk loci.Genetic Dissection of Cardiac Remodeling in an Isoproterenol-Induced Heart Failure Mouse Model.High-Density Genotypes of Inbred Mouse Strains: Improved Power and Precision of Association Mapping.Informatics resources for the Collaborative Cross and related mouse populations DNA Methylation Indicates Susceptibility to Isoproterenol-Induced Cardiac Pathology and Is Associated With Chromatin States.Maximal information component analysis: a novel non-linear network analysis method Cocaine self-administration behavior in inbred mouse lines segregating different capacities for inhibitory control.Genome Sequencing of Chromosome 1 Substitution Lines Derived from Chinese Wild Mice Revealed a Unique Resource for Genetic Studies of Complex Traits.Meta-analysis identifies gene-by-environment interactions as demonstrated in a study of 4,965 mice.Chromosome substitution strains: gene discovery, functional analysis, and systems studies.Lipin-1 and lipin-3 together determine adiposity in vivo.Nicotinamide N-Methyltransferase: More Than a Vitamin B3 Clearance Enzyme.Incorporating comparative genomics into the Design-Test-Learn cycle of microbial strain engineering.

P2860

Q26852866-9A8A3090-FC46-46B5-8501-B32677270A83 Q27325276-1558CC31-E66F-47CA-BB59-19A868AEF1A1 Q27342192-1C75DBD5-A20C-4327-B76A-57B39E3E63D7 Q27347732-8343472F-82B9-47FB-A934-73715BE2EEF9 Q28283087-9C3B2213-524B-47B9-8EE8-304EEE923C7E Q28606497-9A15875A-FA05-4E09-AF4E-149D27B22A95 Q28822408-DE193819-0C83-46AF-9881-F9270D431039 Q30275271-FA567858-3641-4890-8FED-393E94895228 Q30364466-50243343-4F5A-4927-B0B7-262D3B0599EC Q30371907-1F330E92-B7E6-4DEB-85BC-892B68C35631 Q30383534-5CA1A21F-80ED-431E-B1F3-74DD6639BE74 Q30391624-82BCDA5B-0F86-410C-859F-DD1752740F2F Q30412670-BED7B59C-4662-40E0-B3FE-AAD0F0DE7B62 Q30413835-3C8318AD-C28E-4C08-B0B0-C46E34E7C883 Q30458970-EEDF5F79-EB95-4BED-90F3-16EDC8ABF1F2 Q33568411-01BF1766-CEFA-4E10-8961-78CA9BC89754 Q34019187-8F8BD6A2-B558-47C1-8E54-39C0AE1A2F6D Q34631925-D8EDACAA-53F7-4B33-94F6-BE6029DB3CB2 Q34710223-73ABDE26-F2E4-40A1-BBB4-F0579B1648A8 Q34713944-9548D719-8DD3-44DE-B1FA-892F7F524B64 Q35180445-82D44FDD-E552-462F-82C2-3D43541360CF Q35330178-84130DB6-BFCE-4595-A1BC-A032FD26A730 Q35664102-98AFED01-A84E-4E14-865B-9BADD019AACE Q35756379-B104B518-FD2E-41DC-AB74-90C51ABD3EAC Q35843546-72906055-222E-4ACE-8EE0-A5BBE8C76111 Q35883431-90D61AFE-C179-4391-A12D-77918527527D Q35929036-8F6BAFCE-D64B-49AA-A7B0-137B0A990EE1 Q35994508-498117DF-3278-488F-AF58-CA1CA6398D90 Q36069291-7C168A9A-9941-4972-9994-A081E664C088 Q36119879-57444B87-9058-496E-91A5-0E869A5CEC01 Q36248743-52AEB96D-5F9A-4C43-A12D-D694AE9B0AE4 Q36654978-3DEB4A64-5320-4BDB-BAB3-DF8BC7299026 Q36676066-5BF90D08-D689-4D23-9F96-4B26C951C83A Q37164928-DDBB636A-9952-42CA-ACF7-DFF4CD8A02A8 Q37401518-79AC19F4-741D-4D8B-A784-3C5A01AC0C73 Q37458267-F403C186-4475-480D-A8B7-CF8FB20AC00E Q37567595-60C33688-61A8-4810-A86A-8F135CE83428 Q37636439-3F717072-0E85-460B-A4FE-8A060DB61DA1 Q38746034-14744D59-6B03-450F-94A5-2F3F840FB9AA Q39388486-096EF682-A692-4C5E-8F4C-8BD7D4B936C5

P2860

Hybrid mouse diversity panel: a panel of inbred mouse strains suitable for analysis of complex genetic traits.

http://www.wikidata.org/entity/Q30422039

description

2012 nî lūn-bûn

@nan

2012 թուականի Օգոստոսին հրատարակուած գիտական յօդուած

@hyw

2012 թվականի օգոստոսին հրատարակված գիտական հոդված

@hy

2012年の論文

@ja

2012年論文

@yue

2012年論文

@zh-hant

2012年論文

@zh-hk

2012年論文

@zh-mo

2012年論文

@zh-tw

2012年论文

@wuu

name

Hybrid mouse diversity panel: ...... sis of complex genetic traits.

@ast

Hybrid mouse diversity panel: ...... sis of complex genetic traits.

@en

type

label

Hybrid mouse diversity panel: ...... sis of complex genetic traits.

@ast

Hybrid mouse diversity panel: ...... sis of complex genetic traits.

@en

prefLabel

Hybrid mouse diversity panel: ...... sis of complex genetic traits.

@ast

Hybrid mouse diversity panel: ...... sis of complex genetic traits.

@en

P1433

Q30422039-A3AAD291-E1F9-468C-9462-2373CB51F3E6

P1476

Q30422039-2A189161-32CD-4697-997B-5111F8AB4F48

P2093

Q30422039-05C63966-D90D-4F80-A26D-A735E9599CD8

Q30422039-07FD71C7-2984-4641-9A4D-147FD9A54B45

Q30422039-0B5FB8DE-237A-4A7D-997D-B7CDE3DFD9B8

Q30422039-0B68BEC9-2E70-455D-9D06-AE858FFB85EB

Q30422039-1166B0A3-28E6-48C6-A249-30F38B24B89C

Q30422039-1E7E2E51-625B-4CAA-82F0-B00597CC98AA

Q30422039-1EA8D8FC-2814-4C18-88E3-0AEA347BDDC9

Q30422039-26329166-6D56-48FD-9D52-9BAB86DF717B

Q30422039-3B533BE6-CA6F-43B4-9C38-DD4B1CF2F214

Q30422039-3BA764C1-59D4-4F53-A78C-F127E8F53808

P2860

Q30422039-04AF4195-476D-49D9-8E8A-0CF3439063A3

Q30422039-0728D496-80DF-419D-92F4-7AB9620F61BA

Q30422039-0D63A041-9BF9-4252-9A77-7EAA111BEEB3

Q30422039-1A539C34-9D42-41A9-B72F-18A617B14854

Q30422039-1AFDD79F-974A-4CFF-B615-392DE29D69BD

Q30422039-22DD3D42-456E-4000-B3B4-C72393859D80

Q30422039-27957CDE-9AA8-43FA-A8D8-090CD6EEF614

Q30422039-27FD4801-A489-40D3-8100-7FC94BAEC4DC

Q30422039-2803D76A-6FC9-4C7A-ABD1-48E1BDDFD495

Q30422039-297F65CF-36A8-43F3-8073-5B33C9161293

P2888

Q30422039-C75A0B5C-535E-4EBE-8EA3-82F75E2526AF

P304

Q30422039-EF88CB66-0AFE-4B7E-9F19-D9732D09EA88

P31

Q30422039-829E08F1-1A96-43D3-BA59-FA2F9D00B939

P356

Q30422039-00BA79CC-67E9-428D-A248-69B4AE606580

P433

Q30422039-6D781BC7-DD8E-43C6-ABD6-292ECC464A73

P478

Q30422039-2B7488B1-3562-4935-9E73-0F55C1F09191

P50

Q30422039-1CE4BA5A-4242-462F-BE51-6CB3803C2BF0

Q30422039-1E5B3A79-2313-46A0-9EDB-437F4607C17F

Q30422039-3C56A1D0-68FD-40AD-B99D-5AAB15A49D86

Q30422039-5E06C642-1954-41A1-93DB-3000A75B7601

Q30422039-6A605BC8-C573-4D89-9D67-206B171ED73B

Q30422039-7FC5CADB-2075-4AD8-89EA-6A32A57CAE8B

Q30422039-B2413E57-F840-4B88-8039-3B677C98307D

Q30422039-C3927696-5982-4AC1-9B50-5CD7FD93E656

Q30422039-C69FC924-6C83-4F71-8880-A4C53EA42B56

Q30422039-D815379F-16B8-48C5-B847-8CC097EED474

P577

Q30422039-EA60EAA5-AAF9-4788-A2BA-FCFBE9C65944

P5875

Q30422039-AD10F73E-B50A-4700-B29C-D98667EFB446

P698

Q30422039-6022A096-21EE-43C1-9313-FBB0939535DC

P932

Q30422039-1E088D63-C26E-4F3F-B912-985EC507C724

P356

S00335-012-9411-5

P1433

Mammalian Genome

P1476

Hybrid mouse diversity panel: ...... sis of complex genetic traits.

@en

P2093

Anatole Ghazalpour

http://www.w3.org/2001/XMLSchema#string

Atila van Nas

http://www.w3.org/2001/XMLSchema#string

Brian J Bennett

http://www.w3.org/2001/XMLSchema#string

Brian W Parks

http://www.w3.org/2001/XMLSchema#string

Christoph D Rau

http://www.w3.org/2001/XMLSchema#string

Desmond J Smith

http://www.w3.org/2001/XMLSchema#string

Emrah Kostem

http://www.w3.org/2001/XMLSchema#string

Eun Yong Kang

http://www.w3.org/2001/XMLSchema#string

Hooman Allayee

http://www.w3.org/2001/XMLSchema#string

Hyun Min Kang

http://www.w3.org/2001/XMLSchema#string

P2860

Finding the missing heritability of complex diseases

Use of a dense single nucleotide polymorphism map for in silico mapping in the mouse

Systematic survey reveals general applicability of "guilt-by-association" within gene coexpression networks

Mouse genome-wide association and systems genetics identify Asxl2 as a regulator of bone mineral density and osteoclastogenesis

The mystery of missing heritability: Genetic interactions create phantom heritability

Genetic mapping in human disease

Genetic regulation of osteoclast development and function

Mouse genomic variation and its effect on phenotypes and gene regulation

Increasing association mapping power and resolution in mouse genetic studies through the use of meta-analysis for structured populations.

Comparative analysis of proteome and transcriptome variation in mouse.

P2888

s00335-012-9411-5

P304

680-692

http://www.w3.org/2001/XMLSchema#string

P31

scholarly article

P356

10.1007/S00335-012-9411-5

http://www.w3.org/2001/XMLSchema#string

P433

9-10

http://www.w3.org/2001/XMLSchema#string

P478

23

http://www.w3.org/2001/XMLSchema#string

P50

J. David Jentsch

Matteo Pellegrini

Charles R. Farber

Aldons Jake Lusis

P577

2012-08-15T00:00:00Z

http://www.w3.org/2001/XMLSchema#dateTime

P5875

230671267

http://www.w3.org/2001/XMLSchema#string

P698

22892838

http://www.w3.org/2001/XMLSchema#string

P932

3586763

http://www.w3.org/2001/XMLSchema#string